Usefulness of Supportive SMS in Addition to an Internet Based Quit Smoking Program (Www.Slutta.no)

NCT01103427 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4300

Last updated 2013-12-17

No results posted yet for this study

Summary

The purpose of the study is to investigate the effectiveness of a smoking cessation intervention delivered through a technological web based platform (www.slutta.no) with or without a supportive SMS function.

Conditions

  • Smoking Cessation
  • Smoking

Interventions

DEVICE

Internet-based behavioral coaching

Those in the "active comparator arm" will benefit from automated coaching by e-mails with advice, information and support for smoking cessation. These e-mails will be adapted to their personal profile.

DEVICE

SMS based coaching

Those in the experimental SMS based coaching arm will benefit from automated coaching by SMS with advice, information and support for smoking cessation. These SMS's will be adapted to their personal profile.

DEVICE

SMS coaching - UNN recruited

Those in the experimental SMS based coaching arm- UNN recruited - will benefit from automated coaching by SMS with advice, information and support for smoking cessation. These SMS's will be adapted to their personal profile.

DEVICE

SMS craving function - UNN recruited

Those in the experimental SMS based craving/panic function arm - will in addition to the automated coaching by SMS have a panic/craving SMS function. Thus by sending a SMS they will receive instant advise and support for smoking cessation by SMS.

Sponsors & Collaborators

  • The Royal Norwegian Ministry of Health

    collaborator OTHER
  • University Hospital of North Norway

    collaborator OTHER
  • University of Tromso

    lead OTHER

Principal Investigators

  • Inger T Gram, MD, PhD · University of Tromso

  • Bjørn Engum · University Hospital of North Norway

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01103427 on ClinicalTrials.gov